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EC number: 204-578-7 | CAS number: 122-84-9
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

Endpoint summary
Administrative data
Description of key information
Skin Sensitization:
No sensitization reactions were observed in any of the volunteers. Hence, 4-methoxyphenylacetone can be considered to be not sensitizing to human skin.
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- Data is from peer reviewed journals
- Qualifier:
- according to guideline
- Guideline:
- other: as mentioned below
- Principles of method if other than guideline:
- To evaluate skin sensitization potential of 4-methoxyphenylacetone on 25 human volunteers.
- GLP compliance:
- not specified
- Type of study:
- other: Human maximization test
- Justification for non-LLNA method:
- Not specified
- Specific details on test material used for the study:
- IUPAC name: p- methoxyphenylacetone
commen name:1-(p-Methoxyphenyl)-2-propanone
Molecular formula:C10H12O2
Molecular weight :164.203 g/mol
Substance type:organic
InChI:1S/C10H12O2/c1-8(11)7-9-3-5-10(12-2)6-4-9/h3-6H,7H2,1-2H3
Smiles: c1(ccc(OC)cc1)CC(C)=O
physical property: liquid - Species:
- other: Human
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals and environmental conditions:
- no data available
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 4% in petroletum
- Day(s)/duration:
- 48 hours
- Adequacy of induction:
- not specified
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 4% in petrolatum
- Day(s)/duration:
- 48 hours
- Adequacy of challenge:
- not specified
- No. of animals per dose:
- 25 human volunteers
- Details on study design:
- No data available
- Challenge controls:
- No data available
- Positive control substance(s):
- not specified
- Reading:
- 1st reading
- Group:
- test chemical
- Dose level:
- 4% in petrolatum
- Total no. in group:
- 25
- Clinical observations:
- No skin reaction were observed
- Remarks on result:
- no indication of skin sensitisation
- Cellular proliferation data / Observations:
- No skin reaction observed
- Interpretation of results:
- other: not skin sensitizing
- Conclusions:
- No sensitization reactions were observed in any of the volunteers. Hence, 4-methoxyphenylacetone can be considered to be not sensitizing to human skin.
- Executive summary:
A maximization test was carried out to assess the dermal sensitization potential of 4-methoxyphenylacetone in humans.
4-methoxyphenylacetone was applied in concentration 4% in petrolatum to the skin of 25 human volunteers and observed till 48 hours.
No sensitization reactions were observed in any of the volunteers. Hence, 4-methoxyphenylacetone can be considered to be not sensitizing to human skin.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
Skin Sensitization:
Various studies have been investigated for assessing the dermal sensitization potential of 4-methoxyphenylacetone to a greater or lesser extent. The studies are based on in vivo experiments in guinea pigs along with predicted data for target chemical and its structurally similar read across; substances, 4-(p-methoxyphenyl) butan-2-one[CAS: 104-20-1] and 4-methoxybenzyl alcohol[CAS: 105 -13-5].The predicted data using the OECD QSAR toolbox has also been compared with the experimental data.
A maximization test was carried out (Food and Cosmetics Toxicology, Volume 17, Supplement, December 1979, Page 857) to assess the dermal sensitization potential of 4 -methoxyphenylacetone in humans. p-methoxyphenylacetone was applied in concentration 4% in petrolatum to the skin of 25 human volunteers and observed till 48 hours.
No sensitization reactions were observed in any of the volunteers. Hence, 4-methoxyphenylacetone can be considered to be not sensitizing to human skin.
The skin sensitization potential of 4 -methoxyphenylacetone was estimated by SSS (2018) using OECD QSAR toolbox v3.3 with log kow as the primary descriptor. 4 -methoxyphenylacetone was predicted to be not sensitizing to the skin of female guinea pigs.
Skin sensitization effects were also estimated by four different models i.e, Battery, Leadscope, SciQSAR and CASE Ultra used within Danish QSAR database for 4 -methoxyphenylacetone. Based on estimation, no skin sensitization reactions were observed in guinea pigs and humans. Therefore, 4-methoxyphenylacetone was considered to be not sensitizing.
The experimental and estimated results are in agreement with each other indicating a strong possibility ofp-methoxyphenylacetone being not sensitizing to skin.
These results are supported by the experimental study summarized in Food and Cosmetics Toxicology,12, 929, 1974; for the structurally similar read across substance,4-(p-methoxyphenyl) butan-2-one[CAS: 104-20-1]. Application of 5% in petrolatum was made under occlusion to the skin of 25 human volunteers and observed till 48 hours. 4-(p-methoxyphenyl) butan-2-one produced no skin reactions on 25 human volunteers.
Hence, 4-(p-methoxyphenyl) butan-2 -one is considered to be non-sensitizing to human skin.
The above results are further supported by the experimental study summarized in Toxicology, 9 (1978) 261-271; for the structurally similar read across substance, 4-methoxybenzyl alcohol[CAS: 105-13-5]. The study was performed according to modified Draize sensitization test. The preliminary irritation tests were done in Hartley strain albino guinea pigs to determine concentrations suitable for sensitization testing [injection challenge concentration (ICC) and application challenge concentration(ACC) ] In the induction phase, the total dose was administered on one occasion as 4 intradermal injections, each 2.5 times the ICC (2.5X 0.25). Fourteen days later 10 Inbred Hartley strain albino guinea pigs was challenged intradermally in one flank and topically in the other with 0.1 ml aliquots of test substance at the respective ICC and ACC (0.25 and 10 respectively). Twenty-four hours later the reactions were observed. In the absence of sensitization reactions at first challenge the induction and challenge procedures were repeated, and apparent sensitization reactions confirmed 7 days later by a second challenge with controls included.
Based upon the second challenge, it can be concluded that Anisic alcohol (CAS No: 105-13-5) was considered to be not-sensitizing to the skin of albino Hartley guinea pigs at 0.25% ICC and 10% ACC concentrations.
Based on the available data for the target as well as read across substances and applying the weight of evidence approach,4-methoxyphenylacetone was not sensitizing to skin.Comparing the above annotations with the criteria of CLP regulation, test chemical can be classified under the category “Not Classified”.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Available data for the target chemical, 4-methoxyphenylacetone suggests that it is not likely to cause any dermal sensitization to skin.
4-methoxyphenylacetone can be considered to be not sensitizer to skin and can be classified under the category “Not Classified” as per CLP regulation.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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